Jobs at Cellares

The Automation Engineer will develop and optimize automated QC workflows, troubleshoot systems, and support laboratory operations in a GMP environment.

Support design and execution of small-scale and scale-up cell therapy process development experiments using the Cellares platform. Perform cell line maintenance, leukopak processing, gene modification, expansion, cryopreservation, equipment qualification, SOP/report authoring, data analysis, and routine lab tasks to advance automated cell therapy manufacturing processes.

Design and execute experiments (including DOE) to develop and scale cell therapy processes. Collaborate cross-functionally to transfer technologies, author technical documentation, analyze and present results, train staff, troubleshoot processes, and provide technical feedback to engineering and manufacturing teams.

Design and execute cell therapy process development and scale-up experiments, maintain primary cell lines and leukopaks, draft SOPs and batch documentation, analyze process data, troubleshoot semi-automated instruments and LIMS, and implement corrective actions to advance the Cellares automated cell therapy manufacturing platform.

Lead process development and technology transfer for autologous and allogeneic cell therapies, manage and mentor teams, coordinate cross-functional programs, author technical documentation, and evaluate new technologies to optimize the Cellares manufacturing platform.

Lead and develop a manufacturing team to execute cGMP cell therapy production (autologous/allogeneic), ensure compliance, oversee tech transfer, process validation, documentation, audits, continuous improvement, and cross-functional coordination to deliver quality product on schedule.

Lead and execute stabilization, scaling, and continuous improvement of GMP-critical systems (ERP, MES, QMS, PLM, LIMS, integrations). Act as a hands-on player-coach bridging Manufacturing, Quality, Supply Chain, Engineering, and Finance to ensure data integrity, traceability, audit readiness, and operational execution while governing releases, validations, vendor performance, and cross-system issue resolution.

The Quality Control Analyst will perform analytical testing, including in-process, lot release, and stability testing while ensuring compliance with cGMP guidelines. They will also investigate discrepancies and support equipment validation and documentation for regulatory submissions.

The Automation Engineer will develop and optimize lab automation systems, validate QC workflows, and ensure functionality of automated systems for cell therapy manufacturing.

The Director, Operations Finance will oversee FP&A for the Operations organization, driving financial insights, cost forecasts, and operational efficiencies across manufacturing sites globally.

The Director, Corporate FP&A leads financial planning processes, collaborates with functional leaders, and provides analysis to drive financial performance in a biotechnology setting.

The Senior Electrical Engineer will lead electrical design for automation equipment, ensuring compliance and managing design documentation. Responsibilities include collaborating with teams, conduct prototyping, and driving design reviews based on industry standards.

The Director of Enterprise Programs leads client programs in process development, managing teams, overseeing tech transfer, ensuring compliance, and optimizing manufacturing processes for cell therapies.

Lead and support IT/OT operations in a biotech manufacturing lab, ensuring system reliability and compliance with industry regulations.

The Senior Director, Supply Chain leads and develops the Supply Chain organization, implementing strategies for efficiency in materials management, logistics, and production planning within a biotech environment.

The Automation Equipment Engineer will monitor, troubleshoot, and enhance automation equipment, collaborating with teams to resolve issues and improve production systems.

This role involves supporting cell therapy manufacturing processes, leading technology transfers, developing automation, ensuring GMP compliance, and collaborating across departments.

Lead the execution of enterprise AI strategy by operationalizing AI across business systems, focusing on adoption, governance, and measurable ROI in a fast-paced environment.

The Principal Enterprise Data Architect will design and operationalize a data platform, integrating various systems while leading data governance and AI readiness efforts.

Lead MSAT process knowledge, technology transfers, and process automation for cell therapy manufacturing. Drive GMP readiness, process validation, CAPA/FMEA, documentation, root-cause investigations, capacity modeling, and cross-functional stakeholder coordination to scale and improve manufacturing operations.